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首页> 外文期刊>The Korean Journal of Physiology & Pharmacology >Neuroprotective effect of caffeic acid phenethyl ester in 3-nitropropionic acid-induced striatal neurotoxicity
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Neuroprotective effect of caffeic acid phenethyl ester in 3-nitropropionic acid-induced striatal neurotoxicity

机译:咖啡酸苯乙酯对3-硝基丙酸诱导的纹状体神经毒性的神经保护作用

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Caffeic acid phenethyl ester (CAPE), derived from honeybee hives, is a bioactive compound with strong antioxidant activity. This study was designed to test the neuroprotective effect of CAPE in 3-nitropropionic acid (3NP)-induced striatal neurotoxicity, a chemical model of Huntington's disease (HD). Initially, to test CAPE's antioxidant activity, a 2,2'-azino-bis-3-ethylbenzthiazoline-6-sulfonic acid (ABTS) antioxidant assay was employed, and CAPE showed a strong direct radical-scavenging eff ect. In addition, CAPE provided protection from 3NP-induced neuronal cell death in cultured striatal neurons. Based on these observations, the in vivo therapeutic potential of CAPE in 3NP-induced HD was tested. For this purpose, male C57BL/6 mice were repeatedly given 3NP to induce HD-like pathogenesis, and 30 mg/kg of CAPE or vehicle (5% dimethyl sulfoxide and 95% peanut oil) was administered daily. CAPE did not cause changes in body weight, but it reduced mortality by 29%. In addition, compared to the vehicle-treated group, robustly reduced striatal damage was observed in the CAPE-treated animals, and the 3NP-induced behavioral defi cits on the rotarod test were signifi cantly rescued after the CAPE treatment. Furthermore, immunohistochemical data showed that immunoreactivity to glial fibrillary acidic protein (GFAP) and CD45, markers for astrocyte and microglia activation, respectively, were strikingly reduced. Combined, these data unequivocally indicate that CAPE has a strong antioxidant eff ect and can be used as a potential therapeutic agent against HD.
机译:源自蜂巢的咖啡酸苯乙酯(CAPE)是具有强抗氧化活性的生物活性化合物。这项研究旨在测试CAPE在3-硝基丙酸(3NP)诱发的纹状体神经毒性(亨廷顿氏病(HD)的化学模型)中的神经保护作用。最初,为了测试CAPE的抗氧化活性,使用了2,2'-叠氮基双-3-乙基苯并噻唑啉-6-磺酸(ABTS)抗氧化剂测定,CAPE显示出很强的直接自由基清除作用。此外,CAPE还提供了保护,可防止培养的纹状体神经元中3NP诱导的神经元细胞死亡。基于这些观察,测试了CAPE在3NP诱导的HD中的体内治疗潜力。为此,对雄性C57BL / 6小鼠反复给予3NP诱导HD样发病机制,每天给予30 mg / kg的CAPE或溶媒(5%的二甲亚砜和95%的花生油)。 CAPE不会引起体重变化,但可将死亡率降低29%。另外,与媒介物治疗组相比,在CAPE治疗的动物中观察到纹状体损伤明显减少,并且CAPE治疗后明显地挽救了由3NP诱导的轮状试验的行为缺陷。此外,免疫组织化学数据显示,对星形胶质细胞和小胶质细胞活化标记的神经胶质纤维酸性蛋白(GFAP)和CD45的免疫反应性显着降低。综合来看,这些数据明确表明CAPE具有很强的抗氧化作用,可以用作抗HD的潜在治疗剂。

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